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A Dual Origin of the Xist Gene from a Protein-Coding Gene and a Set of Transposable Elements
- Source :
- PLoS ONE, PLoS ONE, Vol 3, Iss 6, p e2521 (2008)
- Publication Year :
- 2008
- Publisher :
- Public Library of Science, 2008.
-
Abstract
- X-chromosome inactivation, which occurs in female eutherian mammals is controlled by a complex X-linked locus termed the X-inactivation center (XIC). Previously it was proposed that genes of the XIC evolved, at least in part, as a result of pseudogenization of protein-coding genes. In this study we show that the key XIC gene Xist, which displays fragmentary homology to a protein-coding gene Lnx3, emerged de novo in early eutherians by integration of mobile elements which gave rise to simple tandem repeats. The Xist gene promoter region and four out of ten exons found in eutherians retain homology to exons of the Lnx3 gene. The remaining six Xist exons including those with simple tandem repeats detectable in their structure have similarity to different transposable elements. Integration of mobile elements into Xist accompanies the overall evolution of the gene and presumably continues in contemporary eutherian species. Additionally we showed that the combination of remnants of protein-coding sequences and mobile elements is not unique to the Xist gene and is found in other XIC genes producing non-coding nuclear RNA.
- Subjects :
- Transposable element
RNA, Untranslated
Genetics and Genomics/Nuclear Structure and Function
lcsh:Medicine
Locus (genetics)
Biology
X-inactivation
Exon
Mice
Tandem repeat
X Chromosome Inactivation
Genetics and Genomics/Epigenetics
Sequence Homology, Nucleic Acid
Animals
lcsh:Science
Gene
Genetics
Multidisciplinary
lcsh:R
Intron
Exons
Genetics and Genomics/Bioinformatics
Tandem Repeat Sequences
DNA Transposable Elements
lcsh:Q
XIST
Female
RNA, Long Noncoding
Genetics and Genomics/Comparative Genomics
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 3
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....1d68b6f710296adc92b79826d22047a3